PureUs

Manufacturer: Winmedia24
Effective date: 2020-06-01
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-05-31 23:16:00

Label at a glance#

ProductPureUs

Active ingredientALCOHOL

Label structure8 sections

Dosage and administration

▪ wet hands thoroughly with product and allow to dry without wiping

Contacts and useful links#

PhoneLabel contact213-713 0095

Websitewww.winmedia24.com

www.winmedia24.com

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Ethyl Alcohol 62%

Purpose

OTC - PURPOSE SECTION

Antimicrobial

Use

INDICATIONS & USAGE SECTION

for hand-washing to decrease on the skin, only when water is not available

Warnings

WARNINGS SECTION

Flammable, Keep away from fire and flames

For External use only

When using this product

▪do not get into eyes

▪if contact occurs, rinse eyes thoroughly with water

Stop use and ask a doctor if

▪irritation and redness develop

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

Directions

DOSAGE & ADMINISTRATION SECTION

▪ wet hands thoroughly with product and allow to dry without wiping

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Distilled water, Glicerine, Vitamin E

SPL UNCLASSIFIED SECTION

• Kills 99.9% of Germs

• Antimicrobial Formula

• Moisturizing

DYE FREE • PHOSPHATE FREE • PARABEN FREE

Made in USA

Distributed by:

Winmedia24, Inc.

Studio City, CA91604

213-713 0095

www.winmedia24.com

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Packaging

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
247835	ethanol 62 % Topical Solution	PSN	1
247835	ethanol 0.62 ML/ML Topical Solution	SCD	1
247835	ethanol 62 % Topical Solution	SY	1
247835	ethyl alcohol 62 % Topical Solution	SY	1

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
78286-725-95	2022-01-28	C162847	48780-1	d6a99b39-7463-a426-e053-dadaa90af4c2	PureUs PREMIUM HAND SANITIZER

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
78286-725-95	PureUs	1922 mL in 1 BOTTLE	LIQUID	1922		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
78286-725	PUREUS (ETHYL ALCOHOL) LIQUID [WINMEDIA24]	1	Legacy NDC, 1 package rows	20200604_fd4f16cc-a7e8-4690-bf7e-342889425951.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

PureUs
Ethyl Alcohol
ALCOHOL
WATER
GLYCERIN
.ALPHA.-TOCOPHEROL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
78286-725	78286-725-95

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ALCOHOL	3K9958V90M	ACTIB
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
.ALPHA.-TOCOPHEROL	H4N855PNZ1	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
43f06f56-a4d3-4f52-9c82-37b3b8e9582b			fd4f16cc-a7e8-4690-bf7e-342889425951	2020-06-01	Warnings	Exact identifier spl id: 43f06f56-a4d3-4f52-9c82-37b3b8e9582b spl set id: fd4f16cc-a7e8-4690-bf7e-342889425951

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.